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Showing 741–750 of 56936 articles for “Art. I-3°”
Any midwife registered on a roll of the Association who carries out midwifery activities in another Member State of the European Community must declare this to the departmental council on whose roll s…
Reasons must be given for all decisions taken by the Association of Midwives in application of this Code of Ethics.Unless otherwise stipulated, decisions taken by the departmental councils may be appe…
Any midwife who ceases to practise must inform the departmental council. The latter acknowledges the decision and informs the national council.
All midwives, when they are entered on the roll, must affirm before the Conseil Départemental de l'Ordre that they are aware of this Code of Ethics and undertake, under oath and in writing, to comply…
The medical permanence of the paediatric haematology intensive care unit in mention 4° of article R. 6123-34-2 is ensured outside day services, by : 1° The presence on site of at least one doctor with…
I. - Authorisation for 3° under the adult critical care modality may only be granted if the holder has a medical unit on site dedicated to cardiology activities. II.- The holder has, on site or by agr…
The travel expenses mentioned in a of 3° of I of article Annexe 4-8 shall be subject to a flat-rate reimbursement: 1° Equal to thirty-two times the 1st class rail mileage tax for each document served,…
After the marketing authorisation has been granted, the marketing authorisation holder must immediately forward to the National Agency for the Safety of Medicines and Health Products, indicating the s…
The Director General of the Agence nationale de sécurité du médicament et des produits de santé may require samples and mock-ups to be submitted when the medicinal product is marketed.
The marketing authorisation issued by the Agence nationale de sécurité du médicament et des produits de santé lapses if it transpires that: 1° That it is not followed by the marketing of the medicinal…
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